DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:4926-55-0
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:4926-55-0
Min.Order:0 Metric Ton
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Type:Manufacturers
inquiryUnique advantages for HC Yellow 2 Cas 4926-55-0 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Powder Storage:Store at RT Package:25kg/drum or as you require Application:Dye
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Cas:4926-55-0
Min.Order:1
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Type:Other
inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
Cas:4926-55-0
Min.Order:1 Gram
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Type:Manufacturers
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Min.Order:5 Kiloliter
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Type:Manufacturers
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Min.Order:1 Kilogram
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:4926-55-0
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiryName: 2-(2-Nitrophenyl)Aminoethanol Synonyms: 2-[(2-nitrophenyl)amino]ethanol CAS:4926-55-0 MF: C8H10N2O3 Appearance:Red crystalline powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application:Syntheses Mat
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Cas:4926-55-0
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:4926-55-0
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiry2-(2-Nitrophenyl)Aminoethanol CAS: 4926-55-0 Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard Shelf life 2 years Storage should be stored i
Cas:4926-55-0
Min.Order:1 Kilogram
FOB Price: $100.0 / 150.0
Type:Other
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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Cas:4926-55-0
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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inquiryProduct name: 2-Nitro-N-(2-Hydroxyethyl)Aniline CAS No.:4926-55-0 Molecule Formula:C8H10N2O3 Molecule Weight:182.17 Purity: 98% Package: 25kg/drum Description:Orange-red crystalline powder Manufacture Standards:Enterprise Standard
Cas:4926-55-0
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryISO9001 Appearance: orange-red crystalline powder Melting Point: 67-72℃ Fe: 20 ppm Max. Pb: 3ppm Max. As : 3ppm Max. Ash: 0.2% max. 2-Fluoronitrobenzene: 50ppm Max. Appearance:orange-red crystalline powder Storage:Store in dry and
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:1 Metric Ton
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryR & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
Cas:4926-55-0
Min.Order:0
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Type:Lab/Research institutions
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Cas:4926-55-0
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
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Negotiable
Type:Lab/Research institutions
inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Conditions | Yield |
---|---|
With potassium carbonate In ethanol for 5h; Reflux; | 99% |
In dimethyl sulfoxide for 1h; Ambient temperature; | 98% |
With potassium carbonate In butan-1-ol Reflux; | 98% |
Conditions | Yield |
---|---|
at 100℃; for 3h; Substitution; | 95.2% |
2-amino-ethanol hydrochloride
ortho-nitrofluorobenzene
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 82℃; for 6h; | 89% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 150℃; for 12h; Green chemistry; | 74% |
Conditions | Yield |
---|---|
at 100℃; for 8h; | 68% |
With potassium carbonate In butan-1-ol Heating; | 54% |
With copper dichloride | |
With copper dichloride | |
With potassium carbonate In ethanol for 8h; Reflux; |
1-amino-2-(2-nitrophenoxy)ethane hydrochloride
A
2-[(2-nitrophenyl)amino]ethanol
B
8-nitro-3,4-dihydro-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With sodium hydroxide; 3,5-dinitrobenzoic acid at -10 - 6℃; for 4h; | A 18% B 57% |
2-Chloronitrobenzene
2,2'-iminobis[ethanol]
A
2-[(2-nitrophenyl)amino]ethanol
B
N,N-bis(2-hydroxyethyl)-2-nitroaniline
C
2-Chloroaniline
D
2,2'-dichloroazobenzene
Conditions | Yield |
---|---|
at 180℃; for 3h; | A 4.6% B 11% C 46% D 0.6% |
1-amino-2-(2-nitrophenoxy)ethane hydrochloride
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
With sodium hydroxide at 33℃; | |
With sodium hydroxide at 33℃; Rate constant; | |
With sodium hydroxide at 33℃; Rate constant; thermal Smiles rearrangement; |
N-(2-hydroxy-ethyl)-2-nitro-benzenesulfonamide
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
With sodium hydroxide |
N-(2-ortho-nitrophenoxyethyl)phthalimide
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 71 percent / aq. HCl / acetic acid / 16 h / Heating 2: 0.01 M aq. NaOH / 33 °C / thermal Smiles rearrangement View Scheme | |
Multi-step reaction with 2 steps 1: 71 percent / aq. HCl / acetic acid / 16 h / Heating 2: 18 percent / aq. NaOH, 3,5-dinitrobenzoic acid / 4 h / -10 - 6 °C View Scheme |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water |
2-Chloroethyl chloroformate
2-nitro-aniline
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
With hydrogenchloride; potassium hydroxide; sulfuric acid; calcium carbonate In anhydrous ethylene glycol dimethyl ether; water |
Conditions | Yield |
---|---|
In water at 80℃; for 8h; Green chemistry; |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethanol; water at 25℃; for 2h; Inert atmosphere; | 100% |
With hydrogen; palladium on activated charcoal In ethanol for 0.5h; Ambient temperature; | 97% |
With 5%-palladium/activated carbon; ammonium formate In methanol at 0 - 25℃; for 1h; | 92% |
5,5-dihydroxy-pyrimidine-2,4,6-trione
2-[(2-nitrophenyl)amino]ethanol
10-(2-hydroxyethyl)isoalloxazine
Conditions | Yield |
---|---|
Stage #1: 2-[(2-nitrophenyl)amino]ethanol With palladium 10% on activated carbon; hydrogen In methanol for 0.666667h; Stage #2: 5,5-dihydroxy-pyrimidine-2,4,6-trione With boric acid In acetic acid at 20 - 80℃; for 19h; Darkness; | 92% |
2-[(2-nitrophenyl)amino]ethanol
methanesulfonyl chloride
2-((2-nitrophenyl)amino)ethyl methanesulfonate
Conditions | Yield |
---|---|
With pyridine Ambient temperature; | 91% |
With pyridine at 20℃; for 2h; Inert atmosphere; Cooling with ice; | 76% |
In pyridine; (2S)-N-methyl-1-phenylpropan-2-amine hydrate |
Conditions | Yield |
---|---|
With ammonium hydroxide; sodium sulfite In methanol at 70℃; for 144h; | 80% |
pyrimidine-2,4,5,6(1H,3H)-tetraone
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
Stage #1: 2-[(2-nitrophenyl)amino]ethanol With palladium 10% on activated carbon; ammonium formate In methanol at 0 - 20℃; for 1h; Stage #2: pyrimidine-2,4,5,6(1H,3H)-tetraone With boric acid; acetic acid at 50℃; for 18h; Darkness; Stage #3: With thionyl chloride at 50℃; for 18h; Darkness; | 80% |
2-[(2-nitrophenyl)amino]ethanol
p-toluenesulfonyl chloride
2-((2-nitrophenyl)amino)ethyl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 48h; Inert atmosphere; | 75% |
ethyl bromide
2-[(2-nitrophenyl)amino]ethanol
N-(β-ethoxyethyl)-o-nitroaniline
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 30 - 35℃; Alkylation; | 55.5% |
2-[(2-nitrophenyl)amino]ethanol
propargyl bromide
2-nitrophenyl-(2-prop-2-ynyloxyethyl)amine
Conditions | Yield |
---|---|
Stage #1: 2-[(2-nitrophenyl)amino]ethanol With sodium hydride In tetrahydrofuran; mineral oil at -20℃; for 0.5h; Stage #2: propargyl bromide In tetrahydrofuran; toluene; mineral oil at 20℃; | 55% |
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
With acetic acid; zinc Erwaermen der Reaktionsloesung mit 3,5-Diphenyl-1,2,4-trion in Aethanol; |
iodobenzene
2-[(2-nitrophenyl)amino]ethanol
2-nitro-N-(2-phenoxyethyl)aniline
Conditions | Yield |
---|---|
With triphenyl phosphite; potassium carbonate 1.) reflux, 6 h; 2.) reflux, 1 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / Pd/C 2: 30 percent / K2CO3; [Cp*IrCl2]2 / xylene / 120 h / 140 °C View Scheme | |
Multi-step reaction with 2 steps 1: Na2S2; H2O 2: concentrated aqueous HCl / 150 - 160 °C View Scheme |
2-[(2-nitrophenyl)amino]ethanol
1-(2-hydroxy-ethyl)-1,4-dihydro-quinoxaline-2,3-dione
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / Pd/C / ethanol / 2585.74 Torr View Scheme |
2-[(2-nitrophenyl)amino]ethanol
3-chloro-1-(2-hydroxy-ethyl)-1H-quinoxalin-2-one
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: H2 / Pd/C / ethanol / 2585.74 Torr 2: phosphorous oxychloride / dimethylformamide / 95 °C View Scheme |
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: H2 / Pd/C / ethanol / 2585.74 Torr 2: phosphorous oxychloride / dimethylformamide / 95 °C 3: acetonitrile / 80 °C View Scheme |
2-[(2-nitrophenyl)amino]ethanol
10-(2-hydroxyethyl)isoalloxazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 91 percent / HCOONH4 / Pd/C / methanol / 25 °C 2: boric acid / acetic acid / 1 h / 50 °C View Scheme | |
Multi-step reaction with 2 steps 1: 5%-palladium/activated carbon; ammonium formate / methanol / 1 h / 0 - 25 °C 2: boric acid; acetic acid / 1 h / 50 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: ammonium formate; palladium on activated charcoal / methanol / 1 h / 0 °C 2: boric acid; acetic acid / 50 °C View Scheme |
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 91 percent / HCOONH4 / Pd/C / methanol / 25 °C 2: boric acid / acetic acid / 1 h / 50 °C 3: SOCl2 / 16 h / 50 °C View Scheme | |
Multi-step reaction with 3 steps 1: 5%-palladium/activated carbon; ammonium formate / methanol / 1 h / 0 - 25 °C 2: boric acid; acetic acid / 1 h / 50 °C / Inert atmosphere 3: thionyl chloride / 16 h / 50 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 3 steps 1: ammonium formate; palladium on activated charcoal / methanol / 1 h / 0 °C 2: boric acid; acetic acid / 50 °C 3: thionyl chloride / 20 h / 50 °C View Scheme |
2-[(2-nitrophenyl)amino]ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 91 percent / HCOONH4 / Pd/C / methanol / 25 °C 2: boric acid / acetic acid / 1 h / 50 °C 3: SOCl2 / 16 h / 50 °C 4: 54 percent / Zn / trifluoroacetic acid / 1 h / Heating View Scheme |
2-[(2-nitrophenyl)amino]ethanol
N-(β-ethoxyethyl)-o-phenylenediamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 55.5 percent / NaH in oil / dimethylformamide / 30 - 35 °C 2: Zn; HCl View Scheme |
2-[(2-nitrophenyl)amino]ethanol
1-(2-ethoxyethyl)-2-chloro-1H-benzimidazole
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 55.5 percent / NaH in oil / dimethylformamide / 30 - 35 °C 2: Zn; HCl 3: Heating 4: POCl3 View Scheme |
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